Variant #0000994962 (NC_000005.9:g.1798943C>T, NM_004553.4:c.-2589C>T (NDUFS6))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1798943C>T
DNA change (hg38) -
Published as MRPL36(NM_032479.3):c.107G>A (p.(Gly36Asp))
ISCN -
DB-ID MRPL36_000006
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NDUFS6 NM_004553.4 -?/. - c.-2589C>T r.(?) p.(=)
MRPL36 NM_032479.3 -?/. - c.107G>A r.(?) p.(Gly36Asp)


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